US6428604B1ExpiredUtilityPatentIndex 89
Hydrometallurgical process for the recovery of nickel and cobalt values from a sulfidic flotation concentrate
Est. expirySep 18, 2020(expired)· nominal 20-yr term from priority
C22B 23/0461C22B 23/0423C22B 3/06C22B 23/043Y02P10/20
89
PatentIndex Score
32
Cited by
27
References
12
Claims
Abstract
A hydrometallurgical process for the recovery of nickel and cobalt values from a sulfidic flotation concentrate. The process involves forming a slurry of the sulfidic flotation concentrate in an acid solution, and subjecting the slurried flotation concentrate to a chlorine leach at atmospheric pressure followed by an oxidative pressure leach. After liquid-solids separation and purification of the concentrate resulting in the removal of copper and cobalt, the nickel-containing solution is directly treated by electrowinning to recover nickel cathode therefrom.
Claims
exact text as granted — not AI-modifiedThe embodiments of the invention in which an exclusive property or privilege is claimed are defined as follows:
1. A process for the extraction, separation and recovery of nickel, cobalt, and copper from a nickel-cobalt-copper-sulfide containing flotation concentrate comprising:
preparing a slurry containing said sulfide containing flotation concentrate and contacting said slurry with an oxygen and chlorine-containing gaseous stream in an atmospheric acid leach stage to thereby generate an oxidative pressure leach feed slurry containing at least about 2 to 40 g/L concentration of chloride ions therein;
subjecting said oxidative pressure leach feed slurry to an oxidative pressure leach under acidic conditions at a temperature ranging between about 100 to 150° C. to selectively leach the majority of the nickel, cobalt and copper therefrom to form a nickel, cobalt, copper-containing oxidative pressure leach solution and an oxidative pressure leach residue;
treating said nickel, cobalt, copper-containing oxidative pressure leach solution after separating the oxidative pressure leach residue therefrom, to separately recover the copper and cobalt, and to remove impurities to thereby form a purified nickel-containing leach solution; and
electrowinning nickel from said purified nickel-containing oxidative pressure leach solution to thereby produce nickel cathode, chlorine, oxygen and sulfuric acid therefrom.
2. The process according to claim 1 comprising finely grinding said sulfidic flotation concentrate to a particulate size ranging between 6 to 30 microns prior to the introduction to said atmospheric acid chlorine leach.
3. The process according to claim 1 wherein the atmospheric leach is conducted at between about 40 to 90° C.
4. The process according to claim 1 including recycling at least a portion of the sulfuric acid produced in the nickel electrowinning step to the atmospheric acid leach.
5. The process according to claim 1 including recycling at least a portion of the chlorine and oxygen produced in the nickel electrowinning step to the atmospheric acid leach.
6. The process according to claim 1 wherein the concentration of chloride ions in the oxidative pressure leach feed slurry ranges between about 5 to 10 g/L.
7. A process for the extraction, separation and recovery of nickel, cobalt, and copper values from a nickel-cobalt-copper-iron sulfide containing sulfidic flotation concentrate comprising:
preparing a slurry containing said sulfidic flotation concentrate and contacting said slurry with an oxygen and chlorine-containing gaseous stream in an atmospheric acid leach at about 40° to 90° C. to thereby generate an oxidative pressure leach feed slurry containing at least about 2 to 40 g/L concentration of chloride ions therein;
subjecting said oxidative pressure leach feed slurry to an oxidative pressure leach under acidic conditions at a temperature ranging between about 100 to 150° C. to selectively leach the majority of the nickel, cobalt and copper therefrom to form a nickel, cobalt, copper-containing leach solution and an oxidative pressure leach residue;
separating said nickel-cobalt-copper-containing oxidative pressure leach solution from said oxidative pressure leach residue;
removing contained copper from said nickel and cobalt-containing oxidative pressure leach solution, neutralizing said copper-depleted nickel and cobalt-containing oxidative pressure leach solution and removing iron therefrom;
purifying said nickel and cobalt-containing oxidative pressure leach solution to thereby remove impurities from the nickel and cobalt-containing oxidative pressure leach solution;
removing cobalt from said nickel and cobalt-containing oxidative pressure leach solution utilizing solvent extraction; and
electrowinning said nickel-containing oxidative pressure leach solution to thereby produce nickel cathode, chlorine, oxygen and sulfuric acid therefrom.
8. The process according to claim 7 comprising finely grinding said sulfidic flotation concentrate to a particle size ranging between about 6 to 30 microns.
9. The process according to claim 7 comprising recycling at least a portion of the sulfuric acid generated in the nickel electrowinning step to said atmospheric acid leach.
10. The process according to claim 7 comprising recycling the oxygen and chlorine generated in said nickel electrowinning step to said atmospheric acid leach.
11. The process according to claim 7 wherein said predetermined concentration of chloride ions in said oxidative pressure leach feed slurry ranges between about 5 to 10 g/L.
12. A process for the preparation of an oxidative pressure leach feed slurry from a nickel-cobalt-copper-containing sulfidic flotation concentrate comprising:
finely grinding said flotation concentrate to a particulate size ranging between about 6 to 30 microns; preparing a slurry containing said finely ground flotation concentrate; and contacting said slurry with an oxygen and chlorine-containing gaseous stream in an atmospheric acid leach to thereby generate a pressure leach feed slurry containing at least about 2 to 40 g/L concentration of chloride ions therein.Cited by (0)
No later patents cite this yet.
References (0)
No backward citations on record.